Breast Cancer Clinical Trial
Official title:
Radiologists' Preference Study - Digital Breast Tomosynthesis
Mammography remains the current standard in the detection of breast cancer. However,
conventional two-view mammography will not detect all cancers. The major limiting factor of
conventional mammography is the presence of superimposed breast tissue that can obscure
clinically significant lesions. It is this limitation that decreases the sensitivity of
mammography and leads to false negative results.
The recent development of digital detectors has allowed imaging technologies such as
tomosynthesis to become clinically feasible. The examination, similar to conventional
mammography with regard to patient positioning and glandular dose, allows acquisition of a
digital data set that can be reconstructed and viewed in multiple sections. The ability of
tomosynthesis to unmask overlapping structures has been shown in preliminary studies to
increase lesion visibility. Used as either a primary imaging modality, or as an adjunct to
screening mammography, tomosynthesis has the potential to provide increased sensitivity and
a lower number of false negative examinations.
The purpose of this study is to compare radiologist impression of digital breast
tomosynthesis to digital mammography with respect to their ability to see and characterize
specific lesion features.
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